Literature DB >> 27113756

ORP5/ORP8 localize to endoplasmic reticulum-mitochondria contacts and are involved in mitochondrial function.

Romain Galmes1, Audrey Houcine1, Alexander R van Vliet2, Patrizia Agostinis2, Catherine L Jackson3, Francesca Giordano3.   

Abstract

The oxysterol-binding protein (OSBP)-related proteins ORP5 and ORP8 have been shown recently to transport phosphatidylserine (PS) from the endoplasmic reticulum (ER) to the plasma membrane (PM) at ER-PM contact sites. PS is also transferred from the ER to mitochondria where it acts as precursor for mitochondrial PE synthesis. Here, we show that, in addition to ER-PM contact sites, ORP5 and ORP8 are also localized to ER-mitochondria contacts and interact with the outer mitochondrial membrane protein PTPIP51. A functional lipid transfer (ORD) domain was required for this localization. Interestingly, ORP5 and ORP8 depletion leads to defects in mitochondria morphology and respiratory function.
© 2016 The Authors.

Entities:  

Keywords:  ORP; endoplasmic reticulum; lipid transfer proteins; membrane contact sites; mitochondria

Mesh:

Substances:

Year:  2016        PMID: 27113756      PMCID: PMC5278607          DOI: 10.15252/embr.201541108

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


  23 in total

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4.  ORP5/ORP8 localize to endoplasmic reticulum-mitochondria contacts and are involved in mitochondrial function.

Authors:  Romain Galmes; Audrey Houcine; Alexander R van Vliet; Patrizia Agostinis; Catherine L Jackson; Francesca Giordano
Journal:  EMBO Rep       Date:  2016-04-13       Impact factor: 8.807

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Journal:  Structure       Date:  2013-06-20       Impact factor: 5.006

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Journal:  Nat Commun       Date:  2014-06-03       Impact factor: 14.919

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3.  ORP5/ORP8 localize to endoplasmic reticulum-mitochondria contacts and are involved in mitochondrial function.

Authors:  Romain Galmes; Audrey Houcine; Alexander R van Vliet; Patrizia Agostinis; Catherine L Jackson; Francesca Giordano
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Review 7.  Bridging the molecular and biological functions of the oxysterol-binding protein family.

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